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Related Concept Videos

Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Related Experiment Video

Updated: Jun 17, 2026

Generalized Psychophysiological Interaction (PPI) Analysis of Memory Related Connectivity in Individuals at Genetic Risk for Alzheimer's Disease
09:38

Generalized Psychophysiological Interaction (PPI) Analysis of Memory Related Connectivity in Individuals at Genetic Risk for Alzheimer's Disease

Published on: November 14, 2017

Genetics Analysis Workshop 16 Problem 2: the Framingham Heart Study data.

L Adrienne Cupples1, Nancy Heard-Costa, Monica Lee

  • 1Department of Biostatistics, Boston University School of Public Health, 801 Massachusetts Avenue, Boston Massachusetts 02118, USA. adrienne@bu.edu.

BMC Proceedings
|December 19, 2009
PubMed
Summary
This summary is machine-generated.

The Framingham Heart Study (FHS) provided rich genetic and longitudinal data for three generations. This resource aids researchers in developing new methods for genome-wide scans and cardiovascular disease risk factor analysis.

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Last Updated: Jun 17, 2026

Generalized Psychophysiological Interaction (PPI) Analysis of Memory Related Connectivity in Individuals at Genetic Risk for Alzheimer's Disease
09:38

Generalized Psychophysiological Interaction (PPI) Analysis of Memory Related Connectivity in Individuals at Genetic Risk for Alzheimer's Disease

Published on: November 14, 2017

Area of Science:

  • Genetics
  • Cardiovascular Disease Research
  • Biostatistics

Background:

  • The Framingham Heart Study (FHS) is a long-term observational study initiated in 1948.
  • Data spans three generations, with repeated measurements for the first two generations.
  • Includes phenotype and genome-wide genotype data.

Purpose of the Study:

  • To provide a comprehensive dataset for analyzing cardiovascular disease risk factors.
  • To facilitate the development and application of new statistical methods for genetic analysis.
  • To enable the study of genome-wide scans using longitudinal family data.

Main Methods:

  • Utilized phenotype data including blood pressure, lipids, diabetes, and coronary heart disease incidence.
  • Incorporated genome-wide genotype data from 550,000 single-nucleotide polymorphisms (SNPs).
  • Employed longitudinal data collection across three generations.

Main Results:

  • The dataset serves as a valuable resource for genetic association studies.
  • Enabled the testing of analytical methods on real-world, complex family data.
  • Facilitated the exploration of genotype-phenotype relationships over time.

Conclusions:

  • The FHS data, combined with genome-wide scans, offers a powerful platform for cardiovascular research.
  • The resource supports advanced statistical genetics and the discovery of novel disease associations.
  • Promotes methodological innovation in analyzing large-scale, longitudinal genetic datasets.